Presented by
Management Forum
Master the essentials of change control in pharmaceutical manufacturing to ensure quality and regulatory compliance. Discover key processes, change types, and industry regulations to maintain high standards.
10 October 2025
+ 17 April 2026 »
from £99
Part of Navigating Risk and Compliance in Pharma series:
Unlock the essential strategies to manage risks and ensure compliance across the entire pharmaceutical supply chain. This dynamic course series dives into critical areas, from mastering deviation management to controlling changes in manufacturing and supply operations. Discover how to maintain top-tier compliance in storage and distribution, with a special focus on third-party logistics (3PL). Equip yourself with the tools to safeguard product quality, meet regulatory standards, and drive continuous improvement in the fast-paced world of pharma.
Managing change control is a crucial element of the pharmaceutical quality management system, as it can impact product quality or regulatory filings. Changes made during pharmaceutical manufacturing and supply operations must be effectively controlled and documented to ensure that their impact, even if minor, is fully understood and addressed.
Maintaining compliance with GxP requirements, change control helps keep processes and systems in a validated state. An effective change control system also ensures consistency in products and services for consumers while demonstrating commitment to regulatory agencies.
This course will explore the crucial steps involved in effectively controlling changes during pharmaceutical manufacturing and supply operations.
This course is part of our GxP training (Good x Practice) course collection, which features a variety of topic areas to ensure you comply with the most recent quality guidelines.
This course is ideal for professionals in the following industries:
Additionally, it is well-suited for professionals in these industries who want to understand the fundamentals of change control and its impact on products and business. It is also beneficial for anyone interested in staying updated on the latest regulations and industry trends affecting pharmaceutical change management.
Dr. Gurpal Singh is an experienced Pharmaceutical Quality Management professional with more than 25 years of experience and a history of success in QA operations management, Quality systems implementation and Continuous improvement. He previously worked in global quality assurance roles within large pharmaceutical companies like MSD and Novartis where he led various quality projects and QA initiatives ensuring compliance with international GxP and regulatory requirements. Gurpal holds a doctorate in Chemistry from Magadh University of India and holds professional certificates in Six Sigma, Quality Auditing and Business Management. He is also a member of International Society of Pharmaceutical Engineering.
NEW higher discounts for multiple bookings - bring your colleagues to make your training budget go further:
Please contact us for pricing if you are interested in booking 5 or more delegates
10 October 2025
Live online
12:00-13:00 UK (London) (UTC+01)
13:00-14:00 Paris (UTC+02)
07:00-08:00 New York (UTC-04)
Course code 16641
Until 05 Sep
Not ready to book yet?
for 7 days, no obligation
17 April 2026
Live online
12:00-13:00 UK (London) (UTC+01)
13:00-14:00 Paris (UTC+02)
07:00-08:00 New York (UTC-04)
Course code 16642
Until 13 Mar
Not ready to book yet?
for 7 days, no obligation
* Early booking discounts may not be combined with other discounts or offers. As such, the discounts for 2nd/3rd/4th delegates are based on the full price; and apply only when booking multiple delegates on the same date.
United Kingdom
Multiple colleagues? See above for details of our discounts for 2, 3, or 4 delegates. For more, talk to one of our training experts to discuss how to: